Control of hydrogen sulfide production in oil fields by managing microbial communities through nitrate or nitrite addition

dc.contributor.advisorVoordouw, Gerrit
dc.contributor.authorHubert, Casey R.J.
dc.date.accessioned2005-08-16T17:03:19Z
dc.date.available2005-08-16T17:03:19Z
dc.date.issued2004
dc.descriptionBibliography: p. 165-175en
dc.description.abstractNitrate or nitrite injection into oil reservoirs during water flooding has the potential to control biological souring, the production of hydrogen sulfide (H2S) by sulfate-reducing bacteria (SRB). Souring control is essential because sulfide is toxic, sulfide precipitates can plug reservoir formations, souring lowers crude oil value, and SRB induce corrosion. Nitrate and nitrite can stimulate heterotrophic nitrate- or nitrite­reducing bacteria (hNRB) and nitrate- or nitrite-reducing, sulfide oxidizing bacteria (NR­SOB). Nitrite also inhibits SRB activity by blocking the sulfate reduction pathway. Continuous up-flow packed-bed bioreactors were inoculated with produced water from the Coleville oil field to establish sulfide-producing biofilms similar to those found in sour reservoirs. Nitrate or nitrite addition to bioreactors indicated that the dose required for hNRB or NR-SOB to control souring depended on the concentration of oil organics. Either mechanism mediates the net removal of oil organics (lactate) with nitrate or nitrite, with lower doses of nitrate required due to its greater oxidative power. Microbial community analysis by reverse sample genome probing (RSGP) revealed that NR-SOB mediated sulfide removal at low nitrate or nitrite concentrations when lactate was still available to SRB and the redox potential was low. At high nitrate doses hNRB oxidized lactate directly, produced nitrite and maintained a high redox potential, thus excluding SRB activity. Facultatively chemolithotrophic Campylobacter sp. strains were isolated from the bioreactors and incorporated into RSGP analyses, revealing their dominance in both NR-SOB- and hNRB-containing communities. The metabolic flexibility of these strains may confer a competitive advantage over obligate chemolithotrophs like Thiomicrospira sp. strain CVO or hNRB that do not have NR-SOB activity like newly isolated Thauera sp. and Rhodobacter sp. strains. A single high dose of nitrite resulted in immediate inhibition of SRB that was independent of hNRB or NR-SOB. Examination of corrosion coupons following bioreactor experiments revealed that nitrite inhibition was the only mechanism that prevented both souring and corrosion. Sulfide elimination by hNRB or NR-SOB resulted in increased pitting corrosion in the region of greatest microbial activity. These findings are instructive for designing souring control treatments and improve understanding of oil field microbial communities.en
dc.format.extentxvii, 212 leaves : ill. ; 30 cm.en
dc.identifier.citationHubert, C. R. (2004). Control of hydrogen sulfide production in oil fields by managing microbial communities through nitrate or nitrite addition (Doctoral thesis, University of Calgary, Calgary, Canada). Retrieved from https://prism.ucalgary.ca. doi:10.11575/PRISM/14739en_US
dc.identifier.doihttp://dx.doi.org/10.11575/PRISM/14739
dc.identifier.isbn0612978621en
dc.identifier.lccAC1 .T484 2004 H83en
dc.identifier.urihttp://hdl.handle.net/1880/41611
dc.language.isoeng
dc.publisher.institutionUniversity of Calgaryen
dc.publisher.placeCalgaryen
dc.rightsUniversity of Calgary graduate students retain copyright ownership and moral rights for their thesis. You may use this material in any way that is permitted by the Copyright Act or through licensing that has been assigned to the document. For uses that are not allowable under copyright legislation or licensing, you are required to seek permission.
dc.titleControl of hydrogen sulfide production in oil fields by managing microbial communities through nitrate or nitrite addition
dc.typedoctoral thesis
thesis.degree.disciplineBiological Sciences
thesis.degree.grantorUniversity of Calgary
thesis.degree.nameDoctor of Philosophy (PhD)
ucalgary.item.requestcopytrue
ucalgary.thesis.accessionTheses Collection 58.002:Box 1508 520492025
ucalgary.thesis.notesUARCen
ucalgary.thesis.uarcreleaseyen
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